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Trial record 52 of 5341 for:    "Depressive Disorder" [DISEASE] AND Behavioral

Pilot Study Assessing Computerized Cognitive Behavioral Therapy for Depression

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ClinicalTrials.gov Identifier: NCT01990053
Recruitment Status : Completed
First Posted : November 21, 2013
Last Update Posted : March 25, 2019
Sponsor:
Information provided by (Responsible Party):
Daniel R. Strunk, Ohio State University

Brief Summary:
Standard treatments for depression in specialty care settings are effective but resources for delivering empirically supported psychotherapies are often limited. Computerized cognitive behavioral therapy (cCBT) is an effective and highly scalable treatment for depression that might help expand services in psychiatric settings, however, little is known about its efficacy in this population. The present study aims to establish the efficacy of a internet-delivered cCBT program ("Beating the Blues") plus email and telephone support for depression in a psychiatric outpatient clinic setting. The secondary aim is to pilot an assessment procedure designed to identify moderators of treatment effectiveness.

Condition or disease Intervention/treatment Phase
Major Depressive Disorder Behavioral: Beating the Blues Not Applicable

Detailed Description:

Currently, outpatient psychiatric settings are plagued by long wait times and are often unable to accommodate all individuals seeking services. Furthermore, a lack of trained therapists in these settings means that many treatment seekers do not have access to empirically supported psychotherapeutic treatments such as cognitive behavioral therapy. "Beating the Blues" (BtB) is a computerized, internet-delivered, cognitive behavioral treatment for depression. BtB is highly scalable and might enable a larger proportion of individuals to receive cognitive behavioral therapy in a psychiatric setting while also reducing therapist time. Although computerized CBT interventions have proven effective in primary care settings, there is no research demonstrating the effectiveness of cCBT in secondary care settings in the United States. Thus the primary goal of the proposed research is to test the efficacy of BtB in a specialty care sample.

Patients presenting to these settings tend to have more severe and complex psychopathology than those presenting to primary care. Although BtB is likely effective, computerized treatments do carry a higher risk of dropout and non-response. Therefore, reliable and valid predictors of response are needed to determine who is most likely to respond to the treatment, versus who is likely to fail or drop out. Thus the second aim of the current proposal is to pilot an assessment procedure containing a number of potential predictors of cCBT response and investigate these predictors for inclusion in a larger validation study.

The current trial is a pilot study with a randomized waitlist control design with optional delayed treatment for individuals randomized to the waitlist condition. For the first phase, the investigators will enroll 90 treatment-seeking adults 18 or older recruited from a pool of individuals seeking outpatient psychiatric services at a hospital clinic. Sixty (n=60) individuals will be assigned immediate treatment group with BtB plus telephone and email support, and n=30 to the waitlist/delayed BtB plus telephone and email support group. Efficacy will be assessed over 8 weeks using the Hamilton Rating Scale for Depression (pre to post treatment) and the PHQ9 (measured at weeks 1-8). There will also be a 1-year follow-up survey with biweekly symptom assessments throughout the year for treatment responders (weeks 9-61). Potential predictors of outcome include demographics, CBT skills, personality measures, cognitive functioning, measures of attitudes and beliefs, social functioning, psychiatric comorbidity and depression illness characteristics, and psychophysiological measures. A second phase will enroll sixty individuals (n=60), who will be assigned immediate treatment group in order to validate the predictive model constructed during Phase 1.


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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 128 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Pilot Study Assessing Computerized Cognitive Behavioral Therapy for Depression
Actual Study Start Date : April 14, 2014
Actual Primary Completion Date : May 3, 2016
Actual Study Completion Date : May 1, 2017

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Beating the Blues
Beating the Blues plus helper support.
Behavioral: Beating the Blues
The BtB program guides patients through a series of 8 fully automated online lessons intended to help them identify and change problematic patterns of thinking and behavior that maintain depression. Support will be provided by licensed professional therapists over the phone or via email.
Other Name: Beating the Blues (BtB)

No Intervention: Waitlist Condition
Eight week waitlist condition group parallel to the immediate treatment condition with optional entrance into the Beating the Blues after the first eight weeks



Primary Outcome Measures :
  1. Change in Hamilton Rating Scale for Depression (HRSD) from 0 to 8 weeks [ Time Frame: week 0, week 8 ]
    The 17-item HRSD, modified to assess atypical symptoms, is a standard interview-administered measure of depressive symptom severity. The HRSD will be administered by study personnel supervised by the Principal Investigator.


Secondary Outcome Measures :
  1. Change in Patient Health Questionnaire-9 (PHQ9) over 8 weeks [ Time Frame: weeks 0-8 ]
    The PHQ9 is a 9-item self-report measure based on the diagnostic criteria for major depression from the Diagnostic and Statistical Manual Fourth Edition (DSM-IV).


Other Outcome Measures:
  1. Change in Generalized Anxiety Disorder-7 (GAD7) over 8 weeks [ Time Frame: weeks 0-8 ]
    The GAD7 is a 7-item self-report measure based on the diagnostic criteria for generalized anxiety disorder from the DSM-IV.

  2. Change in Depression Anxiety and Stress Scale-21 (DASS21) over 8 weeks [ Time Frame: week 0, week 8 ]
    The DASS21 is a 21-item self-report scale measuring symptoms of depression, anxiety, and stress.



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Diagnosis of Major Depressive Disorder (MDD) according to Diagnostic and Statistical Manual Fourth Edition criteria
  • Able and willing to give informed consent
  • Have access to a computer with an internet connection at home

Exclusion Criteria:

  • History of bipolar affective disorder or psychosis
  • Current Axis I disorder other than MDD if it constitutes the predominate aspect of the clinical presentation and if it requires treatment other than that being offered
  • History of substance dependence in the past six months
  • Subnormal intellectual potential (IQ below 80)
  • Clear indication of secondary gain (e.g., court ordered treatment or compensation issues)
  • Current suicide risk or significant intentional self-harm in the last six months sufficient to preclude treatment on an outpatient basis
  • Discharge within six moths from a higher level of care (inpatient, partial hospital, or intensive outpatient treatment)
  • Currently undergoing outpatient psychotherapy
  • Current antidepressant medication treatment if the individual has had a change in medication over the past month or is planning a change in medication during the duration of the study
  • Inability to read and write English

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01990053


Locations
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United States, Ohio
The Ohio State University
Columbus, Ohio, United States, 43210
Sponsors and Collaborators
Ohio State University
Investigators
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Principal Investigator: Daniel R Strunk, PhD Ohio State University

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Responsible Party: Daniel R. Strunk, Associate Professor, Ohio State University
ClinicalTrials.gov Identifier: NCT01990053     History of Changes
Other Study ID Numbers: 2013B0307
First Posted: November 21, 2013    Key Record Dates
Last Update Posted: March 25, 2019
Last Verified: March 2019

Additional relevant MeSH terms:
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Depression
Depressive Disorder
Depressive Disorder, Major
Behavioral Symptoms
Mood Disorders
Mental Disorders